A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7833524



Internal ID13130104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14877435..14877436hg38UCSC Ensembl
Innerchr9:14877418..14877453hg38UCSC Ensembl
Outerchr9:14877417..14877454hg38UCSC Ensembl
chr9:14877433..14877434hg19UCSC Ensembl
Innerchr9:14877416..14877451hg19UCSC Ensembl
Outerchr9:14877415..14877452hg19UCSC Ensembl
chr9:14867433..14867434hg18UCSC Ensembl
Innerchr9:14867451..14867416hg18UCSC Ensembl
Outerchr9:14867415..14867452hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307811
Supporting Variants
SamplesNA11830
Known GenesFREM1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7833524
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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